146 positions on this site are linked to Basal Cell Carcinoma, out of 118,864 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
C2CD6 · rs139504624
See detailed info → Sensitivenear LAMC1 · rs12132262
See detailed info → Sensitivenear LINC02964 · rs4871622
See detailed info → SensitiveVDR · rs7971418
See detailed info → Sensitivenear HLA-DRA · rs28895097
See detailed info → SensitiveTGM3 · rs117226861
See detailed info → Sensitivenear RNU6ATAC37P · rs79483583
See detailed info → SensitiveRPL37A-DT · rs74269473
See detailed info → SensitiveHAUS6 · rs7037714
See detailed info → SensitivePLCL1 · rs1579695
See detailed info → SensitiveEGR3-AS1 · rs117101060
See detailed info → SensitiveATP8B4 · rs8038434
See detailed info → SensitivePPIL3 · rs16835425
See detailed info → Sensitivenear TGM3 · rs117491519
See detailed info → Sensitivenear CPNE1 · rs113203744
See detailed info → SensitiveCNTN5 · rs74603527
See detailed info → Sensitivenear TGM3 · rs142526110
See detailed info → Sensitivenear RNA5SP45 · rs12142181
See detailed info → SensitiveGRHL1 · rs6741117
See detailed info → SensitiveJDP2 · rs2359795
See detailed info →Showing 20 of 146 · page 1 of 8
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.